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CASE REPORT article
Front. Oncol.
Sec. Hematologic Malignancies
Volume 15 - 2025 | doi: 10.3389/fonc.2025.1530852
This article is part of the Research Topic Combination Therapies in Acute Myeloid Leukemia (AML). View all articles
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The prognosis of MECOMr AML is poor, with a 5-year overall survival (OS) rate of less than 10%. This is mostly attributable to the low efficacy of all available therapies and high relapse rates even after allogeneic stem cell transplantation (alloSCT), which remains the only curative approach.We report upfront sequential alloSCT with venetoclax-based preconditioning as a safe and effective treatment for two newly diagnosed and fit MECOMr AML patients. The sequential alloSCT regimen consisted of triple therapy: preconditioning with decitabine and venetoclax on days 1-5 followed by FLAG-Ida and venetoclax on days 6-10. One or three days after preconditioning, the patients underwent busulfan-based myeloablative conditioning and HLA haploidentical or matched related donor stem cell infusion. One month after alloSCT, timely engraftment and complete remission were achieved. At the last follow-up, both patients were in good health and MRD-negative complete remissions after 11 and 17 months after alloSCT, respectively.The safety and efficacy of upfront sequential alloSCT indicate the need to evaluate this approach for adverse risk of AML in clinical trials.
Keywords: Acute myeloid leukaemia (AML), Allogeneic stem cell transplanation, venetoclax (ABT-199, PubChem CID: 49846579), FLAG-Ida, Inversion 3q21q26, MECOM (MDS1 and EV1 complex locus), Hypomethyating agents
Received: 19 Nov 2024; Accepted: 03 Mar 2025.
Copyright: © 2025 Žučenka and Tamutytė. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Andrius Žučenka, Department of Hematology and Oncology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, 03101, Lithuania
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